Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminoindole | HCID 78867 | — |
| Reactant | 4-Chloro-6-iodoquinazoline | HCID 11173809 | — |
| Product | HCID 15521320 | HCID 15521320 | — |
Reaction Steps
JP-A-10-152477 describes a process for preparing a 4-arylaminoquinazoline compound from a quinazolin-4-one, which comprises the steps of chlorinating 4-iodoquinazolin-4-one using an excessive amount of oxalyl chloride to produce 6-iodo-4-chloroquinazoline (intermediate compound), concentrating the reaction product under reducing pressure to isolate the resulting product; reacting the 6-iodo-4-chloroquinazoline with 5-aminoindole to give 6-iodo-4 (5-indolylamino)quinazoline. Unfortunately, the yield is not high. Further, it should be noted that the intermediate compound, i.e., 4-chloroquinazoline compound, shows no satisfactory stability in the presence of water and no satisfactory resistance to heat. Accordingly, the compound should be handled carefully.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08318932B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-8af571ed92d9496799f655e9d5732b86 |
|---|
| Source note | uspto-grants-2012_11 |
|---|